Platelet function in whole blood can be comprehensively evaluated by flow c
ytometry. Flow cytometry can be used to measure platelet reactivity, circul
ating activated platelets, platelet-platelet aggregates, leukocyte-platelet
aggregates, procoagulant platelet-derived microparticles, and calcium flux
. Clinical applications of whole blood flow cytometric assays of platelet f
unction in disease states (e.g., acute coronary syndromes, angioplasty, and
stroke) may include identification of patients who would benefit from addi
tional antiplatelet therapy and prediction of ischemic events. Circulating
monocyte-platelet aggregates appear to be a more sensitive marker of in viv
o platelet activation than circulating P-selectin-positive platelets. Flow
cytometry can also be used in the following clinical settings: monitoring o
f GPIIb-IIIa antagonist therapy, diagnosis of inherited deficiencies of pla
telet surface glycoproteins, diagnosis of storage pool disease, diagnosis o
f heparin-induced thrombocytopenia, and measurement of the rate of thrombop
oiesis. (C) 2000 Academic Press.